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Summary Literature (1)
DOID:0050453 - lissencephaly

Disease Ontology Definition:A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.

Synonyms:

Xenbase Genes : arx, reln, dcx, katnb1, pafah1b1, nde1, cdk5, lamb1, tuba1cl.3, tmtc3, tuba1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018838 - lissencephaly spectrum disorders


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital nervous system abnormality (is_a)